The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

21376–21400 of 114369

  • HighFDA (Devices)·Z-2340-2023·2023-08-16

    Olympus VISERA Tracheal Videoscope reprocessor compatibility and sterilization procedure revision

    Olympus is revising labeling for the VISERA Tracheal Intubation Videoscope to correct equipment compatibility information and update sterilization procedures. The device is no longer compatible with OER-Pro, OER-Elite, and OER-Mini reprocessors; sterilization and cleaning procedures have changed significantly.

    Product
    VISERA Tracheal Intubation Videoscope OLYMPUS LF Type V- For airway management which includes endoscopic observation to access airway anatomy, endotracheal/endobronchial intubation and management.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1385-2023·2023-08-16

    Sweet Alchemy Cookies and Cream ice cream recalled for undeclared allergens

    Sweet Alchemy Cookies and Cream ice cream in cups and pints distributed in Washington is recalled for not declaring egg, milk, and wheat allergens on the label.

    Product
    Sweet Alchemy Cookies and Cream ice cream, distributed in cups and pints. Label declares company name, flavor name, but does not declare ingredients and allergens.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1386-2023·2023-08-16

    Sweet Alchemy Dough or Die ice cream pints lack allergen labeling

    Sweet Alchemy Dough or Die ice cream pints distributed in Washington lack ingredient and allergen declarations on labels. The product contains Egg, Milk, Soy, and Wheat allergens.

    Product
    Sweet Alchemy Dough or Die ice cream, distributed in pints. Label declares company name, flavor name, but does not declare ingredients and allergens.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2357-2023·2023-08-16

    VITROS Troponin I ES Immunodiagnostic Reagent Pack Recalled for Incorrect Wells

    ORTHO-CLINICAL DIAGNOSTICS is recalling VITROS Troponin I ES Reagent Pack due to potential incorrect wells that could generate false negative diagnostic results. Lot 4800 with expiration 10-Jun-2023 is affected.

    Product
    VITROS Immunodiagnostic Products Troponin I ES Reagent Pack
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1387-2023·2023-08-16

    Sweet Alchemy Lemon Custard Ice Cream Recalled Due to Missing Allergen Labeling

    Sweet Alchemy Ice Creamery is recalling Lemon Custard ice cream cups because labels fail to declare ingredients, including the allergens Egg and Milk.

    Product
    Sweet Alchemy Lemon Custard ice cream, distributed in cups. Label declares company name, flavor name, but does not declare ingredients and allergens.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2350-2023·2023-08-16

    Hip stem trial instruments recalled due to excessive removal force

    LINK MP Monoblock hip stem trial instruments may require excessive force to remove after impaction, potentially prolonging surgery or requiring procedural modification.

    Product
    LINK MP Monoblock Hip Stem, Trial Stem Instruments, Size 19-Indicated for patients with Mobility-limiting diseases, fractures or defects of the hip joint or proximal femur Item Number: 136-119/00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2360-2023·2023-08-16

    Angiography systems recalled due to thermal overload in cable connectors

    Siemens ARTIS icono floor angiography systems may experience thermal overload in cable connectors during fluoroscopy, causing burning smell and loss of imaging capability. The recall affects 7 units worldwide.

    Product
    ARTIS icono floor-Angiography systems developed for single and biplane diagnostic imaging and interventional procedures. Material Number: 11327700
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2397-2023·2023-08-16

    Philips MR 7700 Magnetic Resonance System Smoke Detector Interlock Bypass

    Philips MR 7700 MRI systems can have their smoke detector interlock safety mechanism bypassed when power cycled after smoke detection, allowing continued operation despite potential fire hazards.

    Product
    MR 7700 Magnetic Resonance (MR) system, Product Numbers 782120 and 782130 (Upgrade to MR 7700)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1395-2023·2023-08-16

    Undeclared coconut allergen in Sweet Alchemy Vegan Monkey Berry Bash ice cream

    Sweet Alchemy Ice Creamery is recalling Sweet Alchemy Vegan Monkey Berry Bash ice cream distributed in Washington due to undeclared coconut allergen on labels. Affected pints have expiration dates from July 30 to August 21, 2023.

    Product
    Sweet Alchemy Vegan Monkey Berry Bash ice cream, coconut-based product, distributed in pints. Label declares company name, flavor name, but does not declare ingredients and allergens.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1371-2023·2023-08-16

    Bellingham Pasta Co Recalls Semolina Sheets for Undeclared Wheat Allergen

    Bellingham Pasta Co recalls Semolina Sheets because the product contains wheat but the label does not declare it. Affected packages have best-by dates of 7/12, 7/15, or 7/19.

    Product
    Semolina Sheets, net wt. 14oz. Product is packaged in a clear clamshell plastic container. Label declares: Fresh & Hand Crafted Bellingham Pasta Co. Ingredients Semolina Flour, Water, Egg, dusted with Brown Rice Flour. Keep Refrigerated. UPC 8 98975 00218 7.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2362-2023·2023-08-16

    Randox Urea Enzymatic Assay Recall: Falsely Low Test Results Risk

    FDA recalls Randox RX Series Urea test kits because carryover from prior LDL-cholesterol tests may produce falsely low results, up to 11% below accurate values, potentially delaying diagnosis.

    Product
    Randox RX Series Urea Enzymatic Kinetic Assay Ref. Numbers: (1) UR3825 (2) UR3873 (3) UR8334 (4) UR8070 (Modena)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2342-2023·2023-08-16

    Olympus OER-Pro Endoscope Reprocessor Revised Labeling for Equipment Compatibility

    Olympus revised OER-Pro labeling because two endoscope models (LF-V, LF-P) are no longer compatible. Sterilization parameters and cleaning procedures have also changed.

    Product
    Olympus Endoscope Reprocessor OER-Pro-For use in cleaning and high-level disinfection of heat sensitive Olympus flexible endoscopes and their accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2364-2023·2023-08-16

    Medical Device Recall: UroLift Visual Obturator Weld Defect Risk

    The UroLift Visual Obturator has an improperly performed weld that may fracture during use, and the welded area can harbor contamination not removed by standard cleaning. Affected units should not be used.

    Product
    UroLift Visual Obturator, 20Ch-The visual obturator is used with the UroLift¿ system. Instrument for insertion of a cystoscope shaft into the bladder. Model: UL-VO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2395-2023·2023-08-16

    MR Imaging System Smoke Detector Interlock Vulnerable to Bypass via Power Cycling

    Philips Ingenia Elition X MR systems can have their smoke detection safety interlock bypassed by power cycling the equipment. This vulnerability could allow unsafe operation during hazardous conditions.

    Product
    Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia Elition X)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2394-2023·2023-08-16

    HoverMatt air transfer mattress contains undersized unit, increases injury risk

    Stryker's HoverMatt 39-inch inflatable transfer mattresses contain 34-inch units inside, reducing available support surface. This increases friction during patient transfers and raises the risk of skin tears.

    Product
    HoverMatt, 39" W x 78" L, REF: HM39SPU-B
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Food)·F-1389-2023·2023-08-16

    Sweet Alchemy Strawberry Rhubarb Crumble Ice Cream Recalled for Undeclared Allergens

    Sweet Alchemy Strawberry Rhubarb Crumble ice cream distributed in Washington has been recalled because labels do not declare ingredients or allergens including Egg, Milk, and Wheat. Consumers with allergies should not consume this product.

    Product
    Sweet Alchemy Strawberry Rhubarb Crumble ice cream, distributed in pints. Label declares company name, flavor name, but does not declare ingredients and allergens.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1379-2023·2023-08-16

    Bellingham Pasta Bucatini Recalled for Undeclared Wheat Allergen

    Bellingham Pasta Co is recalling Semolina Bucatini pasta because the label fails to declare wheat, a major allergen present in the product. Consumers with wheat allergies risk allergic reaction.

    Product
    Semolina Bucatini, net wt. 13oz. Product is packaged in a clear clamshell plastic container. Label declares: Fresh & Hand Crafted Bellingham Pasta Co. Ingredients Semolina Flour, Water, Egg, dusted with Brown Rice Flour. Keep Refrigerated. UPC 8 98975 00225 5.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1391-2023·2023-08-16

    Sweet Alchemy Toasted Black Sesame Ice Cream Lacks Required Allergen Labeling

    Sweet Alchemy Toasted Black Sesame ice cream pints lack required allergen labeling for Egg, Milk, and Sesame. Affected products were distributed in Washington.

    Product
    Sweet Alchemy Toasted Black Sesame ice cream, distributed in pints. Label declares company name, flavor name, but does not declare ingredients and allergens.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2396-2023·2023-08-16

    Ingenia Elition S MR System smoke detection interlock vulnerable to operator bypass

    Philips Ingenia Elition S MR systems can be circumvented by power cycling to bypass the smoke detection safety interlock that locks after smoke is detected. This could allow continued operation despite fire hazards.

    Product
    Ingenia Elition S Magnetic Resonance (MR) system, Product Numbers 781357 and 782106
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1393-2023·2023-08-16

    Sweet Alchemy Vanilla Cubed Ice Cream Recall: Missing Allergen Declarations

    Sweet Alchemy Vanilla Cubed ice cream sold in Washington was recalled because labels do not declare ingredients, including the allergens Egg and Milk.

    Product
    Sweet Alchemy Vanilla Cubed ice cream, distributed in cups and pints. Label declares company name, flavor name, but does not declare ingredients and allergens.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2361-2023·2023-08-16

    Siemens ARTIS Angiography Systems: Thermal Overload Risk in Cable Connectors

    Siemens has recalled 10 ARTIS angiography systems due to thermal overload hazard in cable connectors. The issue may cause burning smell and loss of imaging functionality, potentially requiring treatment cancellation or system replacement.

    Product
    ARTIS pheno-Angiography systems developed for single and biplane diagnostic imaging and interventional procedures. Material Number: 10849000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1398-2023·2023-08-16

    FDA Recalls Romaine Lettuce Due to Potential Deer Fecal Contamination

    C&E Farms is recalling 8,010 mini-bins of bulk romaine lettuce that may be contaminated with deer feces. The affected lettuce was distributed to retailers in seven U.S. states.

    Product
    Romaine lettuce packed in bulk 45-lb mini-bins
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1400-2023·2023-08-16

    Fresh Creative Foods Caesar Salad Kit Recalled for Potential Deer Feces Contamination

    Fresh Creative Foods Caesar Salad Kit is being recalled due to potential contamination with deer feces. The recall affects 1,210 cases distributed to one facility in Illinois.

    Product
    Fresh Creative Foods Caesar Salad Kit; 3.30 lbs per bag; film bags, individually sealed inside cardboard case; total package size: 6.6 lbs (2 - 3.3 lbs bags); PERISHABLE. KEEP REFRIGERATED
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1374-2023·2023-08-16

    Bellingham Pasta Co Semolina Shells Recalled for Undeclared Wheat Allergen

    Bellingham Pasta Co is recalling Semolina Shells due to undeclared wheat. The product label does not declare wheat, posing a risk to consumers with wheat allergies.

    Product
    Semolina Shells, net wt. 13oz. Product is packaged in a clear clamshell plastic container. Label declares: Fresh & Hand Crafted Bellingham Pasta Co. Ingredients Semolina Flour, Water, Egg, dusted with Brown Rice Flour. Keep Refrigerated. UPC 8 98975 00219 4.
    Category
    Food
    Distribution
    1 state